

FOLLOWUS
a.South China Advanced Institute for Soft Matter Science and Technology, South China University of Technology, Guangzhou 510640, China
b.Laboratory of Advanced Polymeric Materials, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China
c.University of Chinese Academy of Sciences, Beijing 100049, China
d.Sinosteel Anshan Research Institute of Thermo-Energy Co., LTD, Anshan 114044, China
zhouheng@iccas.ac.cn (H.Z.)
wfqiu@scut.edu.cn (W.F.Q.)
Received:20 March 2019,
Revised:2019-6-2,
Accepted:03 June 2019,
Online First:03 September 2019,
Published:2020-01
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Citation: Han, Y.; Tang, D. H.; Wang, G. X.; Sun, Y. N.; Guo, Y.; Zhou, H.; Qiu, W. F.; Zhao, T. Phthalonitrile resins derived from vanillin: synthesis, curing behavior, and thermal properties. Chinese J. Polym. Sci. 2020, 38, 72–83
Yue Han, Dong-Hao Tang, Guang-Xing Wang, et al. Phthalonitrile Resins Derived from Vanillin: Synthesis, Curing Behavior, and Thermal Properties[J]. Chinese Journal of Polymer Science, 2020, 38(1): 72-83.
Citation: Han, Y.; Tang, D. H.; Wang, G. X.; Sun, Y. N.; Guo, Y.; Zhou, H.; Qiu, W. F.; Zhao, T. Phthalonitrile resins derived from vanillin: synthesis, curing behavior, and thermal properties. Chinese J. Polym. Sci. 2020, 38, 72–83 DOI: 10.1007/s10118-019-2311-3.
Yue Han, Dong-Hao Tang, Guang-Xing Wang, et al. Phthalonitrile Resins Derived from Vanillin: Synthesis, Curing Behavior, and Thermal Properties[J]. Chinese Journal of Polymer Science, 2020, 38(1): 72-83. DOI: 10.1007/s10118-019-2311-3.
Vanillin was used as sustainable source for phthalonitrile monomer synthesis
and allyl/propargyl ether moieties were introduced to improve the processability at the minimal cost of thermal properties. The synthesis route was optimized to minimize side-reactions and simplify post-processing
and the monomers were obtained in high purity and good yields. The curing behavior
mechanism
and processability of the monomers were studied
and the thermal properties of cured polymers were evaluated. Of the two monomers
the allyl ether-containing one exhibited a wide processing window of 185 °C
and was mainly cured into phthalocyanine and linear aliphatic structures through self-catalytic curing process. Also
the glass transition temperature was higher than 500 °C. In contrast
the propargyl ether-containing monomer could only be partially cured
and heat resistance was found to be compromised. Compared with traditional petroleum-based phthalonitrile resins
the bio-based monomers could be cured without the addition of catalysts
and improvement in processability was achieved at no cost of thermal performances.
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